批准日期,申请提交历史,通知信,药品说明书,审评文件等信息
提交状态日期 | 提交号 | 审批结论 | 申请内容分类 | 审评优先级;罕用药状态 | 通知信、审评文件、说明书、包装标签 | 备注 |
2024/10/25 |
SUPPL-33(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2022/01/20 |
SUPPL-27(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2022/01/13 |
SUPPL-28(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2022/01/03 |
SUPPL-30(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2020/09/16 |
SUPPL-26(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2019/03/11 |
SUPPL-24(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2019/02/21 |
SUPPL-25(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2018/01/04 |
SUPPL-22(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2016/09/09 |
SUPPL-21(补充) |
Approval |
Labeling |
STANDARD
|
|
Please see www.fda.gov/STIC for labeling requirements on susceptibility test interpretive criteria for systemic antibacterial and antifungal drugs. |
2016/04/11 |
SUPPL-19(补充) |
Approval |
Manufacturing (CMC) |
PRIORITY
|
|
|
2015/11/13 |
SUPPL-20(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2015/11/13 |
SUPPL-18(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2015/08/13 |
SUPPL-17(补充) |
Approval |
Manufacturing (CMC) |
PRIORITY
|
|
|
2015/07/14 |
SUPPL-16(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2015/06/15 |
SUPPL-15(补充) |
Approval |
Manufacturing (CMC) |
PRIORITY
|
|
|
2014/06/16 |
SUPPL-14(补充) |
Approval |
Manufacturing (CMC) |
PRIORITY
|
|
|
2014/01/07 |
SUPPL-13(补充) |
Approval |
Manufacturing (CMC) |
PRIORITY
|
|
|
2012/06/21 |
SUPPL-12(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2012/06/21 |
SUPPL-11(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2010/09/08 |
SUPPL-8(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2009/02/19 |
SUPPL-7(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2008/05/20 |
SUPPL-6(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2008/05/20 |
SUPPL-2(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2006/09/15 |
ORIG-1(原始申请) |
Approval |
Type 1 - New Molecular Entity |
PRIORITY
|
|
|
与本品相关的专利信息(来自FDA橙皮书Orange Book)
与本品治疗等效的药品
活性成分:POSACONAZOLE 剂型/给药途径:SUSPENSION;ORAL 规格:40MG/ML 治疗等效代码:AB
申请号 | 产品号 | 申请类型 | 商品名 | 活性成分 | 剂型/给药途径 | 规格 | 市场状态 | RLD | RS | TE Code | 产品号批准日期 | 申请人 |
022003 |
001 |
NDA |
NOXAFIL |
POSACONAZOLE |
SUSPENSION;ORAL |
40MG/ML |
Prescription |
Yes |
Yes |
AB |
2006/09/15
|
SCHERING |
208773 |
001 |
ANDA |
POSACONAZOLE |
POSACONAZOLE |
SUSPENSION;ORAL |
40MG/ML |
Prescription |
No |
No |
AB |
2020/05/15
|
HIKMA |